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双特异性受体诱饵蛋白通过同时阻断血管内皮生长因子A和C来阻断眼部新生血管形成。

Bispecific receptor decoy proteins block ocular neovascularization via simultaneous blockade of vascular endothelial growth factor A and C.

作者信息

Sargunas Paul R, Ariail Emily, Lima E Silva Raquel, Patil Akash, Zhang Mingliang, Shen Jikui, Lopes Beatriz Silva, Oh Yuseong, McCue Amelia C, Ramasubramanian Ranjani, Stephenson A Carson, Popel Aleksander S, Campochiaro Peter A, Spangler Jamie B

机构信息

Department of Chemical and Biomedical Engineering, Johns Hopkins University Whiting School of Engineering, Baltimore, MD 21218, USA; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.

Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21231, USA.

出版信息

Mol Ther. 2025 Jul 2;33(7):3128-3146. doi: 10.1016/j.ymthe.2025.03.027. Epub 2025 Mar 25.

Abstract

Several debilitating eye diseases that lead to vision loss are driven by ocular neovascularization, which entails abnormal blood vessel growth in the eye. Neovascularization is often induced by the upregulation of vascular endothelial growth factor (VEGF) ligands, which activate angiogenesis through engagement of VEGF receptor (VEGFR) proteins on endothelial cells. Therapeutic interventions that block ocular neovascularization by targeting VEGF ligands, particularly VEGF-A, have revolutionized eye disease treatment. However, a significant population of patients are either non-responders or develop resistance, which can be driven by the upregulation of other VEGF family ligands such as VEGF-C. Here, we engineered two bispecific receptor decoy fusion proteins that incorporate domains of VEGFR-1 and VEGFR-2 for more effective and comprehensive inhibition of VEGF ligands. We demonstrated that our engineered proteins bind all VEGF ligands and can sequester two ligands simultaneously. We further showed that these molecules block VEGF activity to potently inhibit proliferation, migration, and survival of human endothelial cells. Moreover, these receptor decoy proteins significantly reduced ocular neovascularization in two mouse models at doses wherein the current standard-of-care anti-VEGF therapy is ineffective. Collectively, our engineered receptor decoy proteins present a new architecture for VEGF pathway inhibition, offering a promising treatment paradigm for ocular diseases.

摘要

几种导致视力丧失的使人衰弱的眼部疾病是由眼部新生血管形成驱动的,这涉及到眼睛中异常的血管生长。新生血管形成通常是由血管内皮生长因子(VEGF)配体的上调诱导的,这些配体通过与内皮细胞上的VEGF受体(VEGFR)蛋白结合来激活血管生成。通过靶向VEGF配体,特别是VEGF-A来阻断眼部新生血管形成的治疗干预措施彻底改变了眼部疾病的治疗方式。然而,相当一部分患者要么没有反应,要么产生耐药性,这可能是由其他VEGF家族配体如VEGF-C的上调所驱动的。在这里,我们设计了两种双特异性受体诱饵融合蛋白,它们包含VEGFR-1和VEGFR-2的结构域,以更有效和全面地抑制VEGF配体。我们证明了我们设计的蛋白能结合所有VEGF配体,并能同时隔离两种配体。我们进一步表明,这些分子阻断VEGF活性,从而有效抑制人内皮细胞的增殖、迁移和存活。此外,在当前标准护理抗VEGF治疗无效的剂量下,这些受体诱饵蛋白在两种小鼠模型中显著减少了眼部新生血管形成。总的来说,我们设计的受体诱饵蛋白为VEGF通路抑制提供了一种新的结构,为眼部疾病提供了一种有前景的治疗模式。

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